• 한국토양환경학회지
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• 제4권2호
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• pp.77-86
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• 1999

난분해성 유기물로 오염된 토양/지하수의 복원을 위하여 계면활성제를 이용 시 토양에 흡착된 계면활성제가 미치는 영향을 평가하기 위하여 소수성 유기물의 흡수현상을 시험하였다. 흡착된 계면활성제에 대한 유기오염물의 흡수계수($K_ss$)는 평형상태에서의 계면활성제 흡착곡선과 밀접한 관계를 이루었다. 즉, 낮은 농도의 흡착에 대한 $K_ss$는 가장 큰 값을 보였고 흡착량이 증가할수록 감소하는 경향을 보였다. SDS에 대한 $K_ss$값은 미셀분배계수($K_mic$) 보다 컸으며 Tween 80에 대해서는 가장 낮은 흡착농도에서의 $K_ss$값을 제외하고 모든 농도 범위에서 $K_{mic}$ 보다 큰 값을 보였다. 유기오염물의 분배계수 또한 계면활성제의 주입량에 따라 변하며 주입되는 계면활성제 농도가 증가할수록 증가하며 일정 농도 이상의 계면활성제 농도에서 감소하기 시작하였다. 이러한 결과는 미셀과 흡착된 상태의 계면활성제 사이에서 오염물 흡수를 위한 상호경쟁에 기인되는 것으로 판단된다. 결론적으로 토양에의 계면활성제 흡착은 유기오염물의 지체현상을 증가시키는 역할을 하여 계면활성제를 이용한 유기오염물 제거 시 저해영향을 미치므로 각 오염부지의 특성별로 유기오염물의 분포를 계면활성제 주입량의 함수로써 평가하는 단계가 선행되어야 한다.다.

• 한국환경과학회지
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• 제19권5호
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• pp.549-563
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• 2010

The environmental behaviors of polycyclic aromatic hydrocarbons (PAHs) are mainly governed by their solubility and partitioning properties on soil media in a subsurface system. In surfactant-enhanced remediation (SER) systems, surfactant plays a critical role in remediation. In this study, sorptive behaviors and partitioning of naphthalene in soils in the presence of surfactants were investigated. Silica and kaolin with low organic carbon contents and a natural soil with relatively higher organic carbon content were used as model sorbents. A nonionic surfactant, Triton X-100, was used to enhance dissolution of naphthalene. Sorption kinetics of naphthalene onto silica, kaolin and natural soil were investigated and analyzed using several kinetic models. The two compartment first-order kinetic model (TCFOKM) was fitted better than the other models. From the results of TCFOKM, the fast sorption coefficient of naphthalene ($k_1$) was in the order of silica > kaolin > natural soil, whereas the slow sorbing fraction ($k_2$) was in the reverse order. Sorption isotherms of naphthalene were linear with organic carbon content ($f_{oc}$) in soils, while those of Triton X-100 were nonlinear and correlated with CEC and BET surface area. Sorption of Triton X-100 was higher than that of naphthalene in all soils. The effectiveness of a SER system depends on the distribution coefficient ($K_D$) of naphthalene between mobile and immobile phases. In surfactant-sorbed soils, naphthalene was adsorbed onto the soil surface and also partitioned onto the sorbed surfactant. The partition coefficient ($K_D$) of naphthalene increased with surfactant concentration. However, the $K_D$ decreased as the surfactant concentration increased above CMC in all soils. This indicates that naphthalene was partitioned competitively onto both sorbed surfactants (immobile phase) and micelles (mobile phase). For the mineral soils such as silica and kaolin, naphthalene removal by mobile phase would be better than that by immobile phase because the distribution of naphthalene onto the micelles ($K_{mic}$) increased with the nonionic surfactant concentration (Triton X-100). For the natural soil with relatively higher organic carbon content, however, the naphthalene removal by immobile phase would be better than that by mobile phase, because a high amount of Triton X-100 could be sorbed onto the natural soil and the sorbed surfactant also could sorb the relatively higher amount of naphthalene.

• 상하수도학회지
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• 제20권3호
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• pp.389-395
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• 2006

The use of pine bark, a natural adsorbent prepared from Korean Red Pine (Pinus densifloral), was studied for its adsorption behavior of lead ion from aqueous solution. Adsorption experiments were carried out on lead ion concentrations of 10mg/L. Adsorption of lead ion could be described by both Langmuir and Freundlich adsorption isotherms. Treatment of the bark with nitric acid greatly increased initial adsorption rate, and equilibrium sorption capacity increased by approximately 48%. A pseudo second-order kinetic model fitted well for the kinetic behavior of lead ion adsorption onto the bark. Acid-treated bark demonstrated its adsorption capacity quite close to that of granular activated carbon. Results of this study indicated that ion exchange and chelation were involved in the adsorption process.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2001년도 추계학술발표회
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• pp.115-119
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• 2001

Contaminant retardation factor is derived from the colloidal and contaminant transport equations for a four-phase porous medium: an aqueous phase, two mobile colloidal phases, and a solid matrix. It is assumed that the contaminant sorption to solid matrix and colloidal particles and the colloidal deposition on solid matrix follow the linear isotherms. The behavior of the contaminant retardation factor in response to the change of model parameters is examined employing the experimental data of Magee et al. (1991) and Jenkins and Lion (1993). In the four-phase system, the contaminant retardation factor is determined by both the contaminant association with solid matrix and colloidal particles and the colloidal deposition on solid matrix. The contaminant mobility is enhanced when the affinity of contaminants to mobile colloids increases. In addition, as the affinity of colloids to solid matrix decreases, the contaminant mobility increases.

• 한국물환경학회지
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• 제25권3호
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• pp.370-374
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• 2009

Adsorption characteristics of glass fibers, obtained from the spent lithium primary batteries recycling process, were investigated for the removal of Acid Red 27 dye from aqueous solution. The batch data clearly showed that increasing the initial sorptive concentration apparently enhanced the amount adsorbed and the uptake process followed the pseudo-second order rate model. The equilibrium adsorption data at different initial sorptive concentrations were fitted well to Freundlich and Langmuir adsorption isotherms. Moreover, the increase in temperature, favored the uptake of dye on this solid, indicated the process was endothermic in nature. Further, using the temperature dependence sorption data obtained at different temperatures was used to estimate various thermodynamic parameters.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2000년도 추계학술대회
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• pp.196-201
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• 2000

The influence of adsorption on cadmium toxicity to soil microorganisms in smectite-rich soils and sediments was quantified as a function of solution and sorbent characteristics. Adsorption and surface complexation experiments were conducted to infer Cd sorption mechanisms to a reference smectite and three fractions of a Veritsol soil, and to elucidate the effects of the surface complexation on Cd bioavailability and toxicity in soils and sediments. Cadmium adsorption isotherms conformed to the Langmuir adsorption model, with adsorptive capacities of the different samples dependent on their characteristics. Equilibrium geochemical modeling (MINTEQA2) was used to predict the speciation of Cd in the soil suspensions using Langmuir and Triple Layer surface complexation models. The influence of adsorption and surface complexation on cadmium toxicity to soil microorganisms was assessed indirectly through the relative change in microbial hydrolysis of fluorescein diacetate (FDA) as a function of total Cd concentration and sorbent characteristics. Adsorption decreased the toxicity of Cd to soil microorganisms. Inner-sphere complexation is more effective than outer-sphere complexation in reducing the bioavailability and toxicity of heavy metals in soils and sediments.

• 한국철도학회:학술대회논문집
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• 한국철도학회 2009년도 춘계학술대회 논문집
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• pp.1530-1535
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• 2009

Moisture evaporates, when concrete is exposed to fire, not only at concrete surface but also at inside the concrete to adjust the equilibrium and transfer properties of moisture. The equilibrium properties of moisture are described by means of water vapor sorption isotherms, which illustrate the hysteretical behavior of materials. In this paper, the prediction method of the moisture distribution inside the high strength concrete members under the high temperature is presented. Finite element method is employed to facilitate the moisture diffusion analysis for any position of member. And the moisture diffusivity model of high strength concrete by high temperature is proposed. To demonstrate the validity of this numerical procedure, the prediction by the proposed algorithm is compared with the test result of other researcher. The proposed algorithm shows a good agreement with the experimental results including the vaporization effect inside the concrete.

• Bulletin of the Korean Chemical Society
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• 제33권11호
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• pp.3711-3718
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• 2012

Here, we report a chain-length dependent morphology and pore structure tailing of mesoporous silica templated from organogels, which is formed by primary alkylamine and ethylene glycol at room temperature. As the chain length of alkylamine changes from 12 to 18, the resulted materials exhibit a morphology change from layers to spheres and platelets, respectively. SEM and TEM observation revealed that these shapes appear to be inherited from their parent organogels. Further pore structure characterization by nitrogen sorption analysis demonstrates that all the resulted silicas exhibit typical IV isotherms indicative of uniform mesopores, and their pore sizes are dependent on the chain length of alkylamine used.

• 농업과학연구
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• 제27권2호
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• pp.135-140
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• 2000

토양내에서 황산이온의 이동성은 산화환원전위, 토양광물 특성, pH, 그리고 환산이온과 토양입자 표면에 흡착에 관여하는 타 음이온들에 의해 영향을 받는다고 알려져 있 다. 제시된 황산이온의 흡착 기작은 토양입자 표면과 수용성상태의 음이온간의 상관 관계를 나타낸 것이다. 그러므로 흡 탈착연구로 부터 얻어진 적정한 계수를 적용함으로서 다중 이온이 존재하는 토양내에서의 일반적 등온흡착 곡선을 적용할 수 있는 이 동모형은 실험적 접근 방법을 수용하게 된다.

• 대한자원환경지질학회:학술대회논문집
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• 대한자원환경지질학회 2003년도 춘계 학술발표회 논문집
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• pp.61-65
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• 2003

Zinc occurs in the nature as sulfide, carbonate, silicate, and oxide. In natural water, zinc is generally in the form of the divalent cation $Zn^{2+}$ as well as in the form of fairly weakly bound complexes. Human activities introduce zinc ion to the hydrosphere in many ways. The zinc complexes in the aqueous environment are accumulated not only in aquatic organisms but also in human body ultimately through physico-chemical and/or biological processes. (omitted)